chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5155917495155917496AG25GENICheterozygous55931256
5155917499155917500TG23GENICheterozygous55804150
5155917538155917539AG18GENICheterozygous55804151
5155917546155917547TC18GENICheterozygous55804152
5155917548155917549CA20GENICheterozygous55804153
5155917573155917574TC19GENICheterozygous55804154
5155917640155917641TA24GENICheterozygous55804155
5155917670155917671CT25GENICheterozygous55804156
5155917702155917703GT26GENICheterozygous55804157
5155917716155917717AC23GENICheterozygous55804158
5155917733155917734GA21GENICheterozygous55804159
5155917750155917751AC20GENICheterozygous55804160
5155917771155917772TG17GENICheterozygous55804161
5155917917155917918GC13GENICheterozygous56070949
5155917921155917922TC13GENICheterozygous55931264
5155918646155918647C-19GENICheterozygous55804167
5155919101155919105AGGG----9GENICheterozygous55804168
5155919101155919103AG--9GENICpossibly homozygous55804169
5155919519155919520CA20GENIChomozygous55804170